Eva C D Stewart, Naoto Jimi, Camille Moreau, Helena Wiklund, Thomas G Dahlgren, Adrian G Glover
{"title":"Novel deep-sea commensalism: a new genus and two new species of Myzostomida from the abyssal Pacific Ocean.","authors":"Eva C D Stewart, Naoto Jimi, Camille Moreau, Helena Wiklund, Thomas G Dahlgren, Adrian G Glover","doi":"10.1071/IS25078","DOIUrl":null,"url":null,"abstract":"<p><p>Symbiotic relationships are ubiquitous across nature and play key roles in the maintenance of biodiversity and ecosystem function. The Myzostomida are an enigmatic clade of marine annelids that live as obligate symbionts on or inside their predominantly echinoderm hosts. Species of myzostomid have diverse morphologies and lifestyles, ranging from cyst and gall forming, to parasitic host eating, and free-living ectocommensalism. Largely described from shallow tropical waters, there is currently limited information on myzostomids from the deep sea. Here we describe, using integrated morphological and molecular data, the first genus and two species of myzostomid from the abyssal seafloor, found living ectocommensally on porcellanasterid starfish from 3490 to 4362 m deep in the central and North Pacific Ocean. Molecular phylogenetic analyses using both nuclear (18S rRNA, H3) and mitochondrial (COI, 16S rRNA) markers recovered Myrmekimyzostomumgen. nov. as monophyletic, and the sole commensal genus in a clade of parasitic species associated with asteroids and ophiuroids. Trait-mapping across the phylogeny suggests the ancestral myzostomid form likely lived ectocommensally on stalked crinoids, with parasitism emerging multiple times in their evolutionary history. These new taxa underline the substantial ecological and evolutionary novelty that can be found in the deep sea. Zoobank: urn:lsid:zoobank.org:pub:332B8B95-F390-4D9F-B1FE-E9E4D433E24C.</p>","PeriodicalId":54927,"journal":{"name":"Invertebrate Systematics","volume":"40 4","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2026-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Invertebrate Systematics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1071/IS25078","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Symbiotic relationships are ubiquitous across nature and play key roles in the maintenance of biodiversity and ecosystem function. The Myzostomida are an enigmatic clade of marine annelids that live as obligate symbionts on or inside their predominantly echinoderm hosts. Species of myzostomid have diverse morphologies and lifestyles, ranging from cyst and gall forming, to parasitic host eating, and free-living ectocommensalism. Largely described from shallow tropical waters, there is currently limited information on myzostomids from the deep sea. Here we describe, using integrated morphological and molecular data, the first genus and two species of myzostomid from the abyssal seafloor, found living ectocommensally on porcellanasterid starfish from 3490 to 4362 m deep in the central and North Pacific Ocean. Molecular phylogenetic analyses using both nuclear (18S rRNA, H3) and mitochondrial (COI, 16S rRNA) markers recovered Myrmekimyzostomumgen. nov. as monophyletic, and the sole commensal genus in a clade of parasitic species associated with asteroids and ophiuroids. Trait-mapping across the phylogeny suggests the ancestral myzostomid form likely lived ectocommensally on stalked crinoids, with parasitism emerging multiple times in their evolutionary history. These new taxa underline the substantial ecological and evolutionary novelty that can be found in the deep sea. Zoobank: urn:lsid:zoobank.org:pub:332B8B95-F390-4D9F-B1FE-E9E4D433E24C.
期刊介绍:
Invertebrate Systematics (formerly known as Invertebrate Taxonomy) is an international journal publishing original and significant contributions on the systematics, phylogeny and biogeography of all invertebrate taxa. Articles in the journal provide comprehensive treatments of clearly defined taxonomic groups, often emphasising their biodiversity patterns and/or biological aspects. The journal also includes contributions on the systematics of selected species that are of particular conservation, economic, medical or veterinary importance.
Invertebrate Systematics is a vital resource globally for scientists, students, conservation biologists, environmental consultants and government policy advisors who are interested in terrestrial, freshwater and marine systems.
Invertebrate Systematics is published with the endorsement of the Commonwealth Scientific and Industrial Research Organisation (CSIRO) and the Australian Academy of Science.